5-substituted-1,3,4-thiadiazole-2-carboxaldehydes

ABSTRACT

THIS INVENTION RELATES TO NOVEL 5-AMINO, 5-ACETAMIDO AND 5-NITRO-1,3,4-THIADIAZOLE-2-CARBOXALDEHYDES AND THEIR DERIVATIVES. THESE COMPOUNDS ARE USEFUL AS ANTIBACTERIAL OR ANTIFUNGAL AGENTS AND ARE IMPORTANT INTERMEDIATES FOR THE PREPARATION OF 2-AMINO-5-(1-SUBSTITUTED-2-IMIDAZOLYL)-1,3,4-THIADIAZOLES.

United States Patent 01' Iioe 3,598,830 Patented Aug. 10, 1971 3,598,830 S-SUBSTITUTED-1,3,4-THIADIAZOLE-2- CARBOXALDEHYDES Gerald Berkelhammer, Princeton, and Gore Asato, Titusville, N.J., assignors to American Cyanamid Company,

Stamford, Conn. No Drawing. Filed Oct. 11, 1968, Ser. No. 767,004 Int. Cl. C07d 91/62 US. Cl. 260-302D 4 Claims ABSTRACT OF THE DISCLOSURE This invention relates to novel S-amino, 5-aceta1nido and 5-nitro-1,3,4-thiadiazole-2-carboxaldehydes and their derivatives. These compounds are useful as antibacterial or antifungal agents and are important intermediates for the preparation of 2-arnino-5-(l-substituted-Z-imidazolyl)-1,3,4-thiadiazoles.

SUMMARY OF THE INVENTION The present invention relates to novel thiadiazole compounds, a method for their preparation and a method of use for controlling bacteria and fungi, particularly plant pathogenic bacteria and fungi. More particularly, the novel compounds of the invention have the formula:

j H R \S/R1 wherein R is selected from the group consisting of amino,

nitro and lower alkanoylamino and R is selected from the group consisting of methyl, formyl,

and

with the proviso that when R is methyl R is nitro.

In the preparation of the present compounds as shown in the flowsheets and examples hereinafter set forth three essential starting materials are used. The first of these is S-nitro-l,3,4-thiadiazole-Z-carboxaldehyde, the product of 'Examples 1 and 4, and described in the flow diagrams as compound (IV). The second is S-amino-1,3,4-thiadiazole- Z-carboxaldehyde, the product of Example 3, identified as compound (III) in the flow diagrams and S-acetamidol,3,4-thiadiazole-Z-carboxaldehyde, the product of Example 11 and referred to in the flow diagrams as compound (XI).

In accordance with the invention and referring to flow diagram 1, 5 nitro-1,3,4-thiadiazole-Z-carboxaldehyde (IV) can be prepared by oxidation of 2-methyl-5-nitro- 1,3,4-thiadiazole (I) at high temperature. The reaction is preferably carried out in the presence of an inert organic solvent and employing an oxidizing agent such as, for example, selenium dioxide. Said compound (IV) may also be prepared from S-amino-l,3,4-thiadiazole-2-carboxaldehyde (III) by formation of the aldehyde diazonium salt followed by reaction with excess alkali metal nitrite in the presence of a copper catalyst.

The 5-nitro-2-thiadiazole-carboxaldehyde (IV) may then be converted to 3-{[(S-nitro-1,3,4-thiadiazol-2-yl) methylene] amino}-2-oxazolidinone (V), l-{ (S-nitro- 1,3,4 thiadiazol 2-yl)methylene]amino}-2-imidazolidinone (VI) or S-nitro-l,3,4-thiadiazole-2-carboxaldehyde thiosemicarbazone (VII) by reaction of the above said carboxaldehyde (IV) with 3-amino-2-oxazolidinone, 1- aminoQ-imidazolidinone or thiosemicarbazide, respectively. The reactions are preferably conducted in an alcoholic or aqueous-alcoholic medium at an elevated temperature, generally between about 70 C. and C. and under slightly acidic conditions. Mineral acids such as hydrochloric and sulfuric acid are well adapted to use in these reactions.

Similarly, treatment of 5-amino-l,3,4-thiadiazole-2- carboxaldehyde (III) (Flow Diagram II) or S-acetamido- 1,3,4-thiadiazole-Z-carboxaldehyde (XI) (Flow Diagram III) with l-amino-2-imidazolidinone, 3-amino-2-oxazolidinone or thiosemicarbazide, under acid conditions at an elevated temperature, yields respectively, the corresponding l-{ (S-aminol ,3 ,4-thiadiazol-2-yl) methylene] amino}- Z-imidazolidinone (XII),

3-{ (S-amino-l,3,4-thiadiazol-2-yl)methylene] amino}- 2-oxazolidinone (XV),

S-amino-1,3,4-thiadiazolecarboxaldehyde thiosemicarbazone (XVII), and

1-{ (S-acetamido-l ,3 ,4-thiadiazol-2-yl methylene] amino}-2-imidazolidinone (XIII),

3-{ (S-acetamido-1,3,4-thiadiazol-2-yl)methylene] amino}-2-oxazolidinone (XIV), and

S-acetamido-1,3,4-thiadiazole-Z-carboxaldehyde thiosemicarbazone (XVI).

Cyclization of S-nitro-1,3,4-thiadiazole-Z-carboxaldehyde thiosemicarbazone (VII), (Diagram I), S-amino- 1,3,4 thiadiazolecarboxaldehyde thiosemicarbazone (XVII), (Diagram 11), and S-acetamido-1,3,4-thiadiazole- Z-carboxaldehyde thiosemicarbazone (XVI), (Diagram III), to the corresponding aminothiadiazoles can then be achieved by treatment of said thiosemicarbazones with an oxidative cyclizing agent such as ferric ammonium sulfate, ferric chloride or ferric sulfate, at an elevated temperature preferably between about 70 C. and 115 C. in water or aqueous alcohol.

Treatment of the cyclized bis amino compound (XVIII) (Diagram II) with acetic anhydride at high temperature, yields the corresponding bis acetamido compound (XIX).

When the S-nitro- (IV) or S-acetamido-1,3,4-thiadazole carboXaldehydes (XI) are reacted with quinaldine and acetic anhydride under acid conditions and high temperature the corresponding thiadiazol-Z-yl vinyl quinolines, (XX) and (XXI) respectively, are formed. However, the S-amino carboxaldehyde (III) does not undergo the same reaction to form the corresponding S-amino vinyl quinoline, but rather, yields the S-acetamido vinyl quinoline (XXI) which is converted by acid hydrolysis to the 2-[2-(5-amino 1,3,4 thiadiazol-2-yl)vinyl]quinoline (XXII), (Diagram III).

In Flow Diagram (II) it can be seen that 5-amino-1,3, 4-thiadiazole-2-carboxaldehyde (III) may be obtained by first refluxing p-nitrobenzaldehyde with 2 acetamido-5- methylthiadiazole in acetic anhydride to obtain p-(S- acetamido 1,3,4-thiadiazol-2-yl)-p-nitrostyrene (II) and ozonizing such product in the presence of ethyl acetate to yield a crude product containing 5 acetamido-1,3,4- thiadiazole 2 carboxaldehyde (XI) which may be hydrolyzed to 5 amino-1,3,4-thiadiazole-2-carboxaldehyde l NH XIII The compounds of the present invention are useful as antibacterial and antifungal agents. They find utility in such areas as treatment of industrial process waters used for cooling equipment and in paper manufacture to control slimes. Generally about to 500 p.p.m. of the compounds of the present invention are effective for this purpose. As indicated, these compounds are also useful for protecting fabrics, textiles, leather and the like as well as agronomic crops, both growing and harvested, from the deleterious effects of these organisms.

In practice the compounds of the invention may be formulated with both solid and liquid diluents and applied in the form of dusts and sprays to the materials or plants for which protection is sought.

Dust formulations are generally prepared by admixing about 1% to by weight of active compound with a finely divided carrier such as kaolin, attapulgite, diatomaceous earth, talc or the like and can be applied with conventional dusting apparatus. For protection of growing plants generally about /2 lb. to 8 lbs. per acre of active ingredient is sufiicient but somewhat higher rates may be employed if so desired.

Wettable powder formulations which are generally dispersed in an inexpensive liquid carrier, such as water or deodorized kerosene, for spray application, are usually prepared by admixing about 25% to 90% by Weight of active ingredient with about 5% to 25 of a solid diluent, as described above with regard to dust formulation, about 1% to 3% of a wetting agent and about 2% to 5% of a dispersant. For application to crops, the wettable powder is dispersed in water in suflrcient amount to provide about /2 lb. to 2 lbs. of active ingredient per 100 gallons of water and applied at the rate of about 100 to 400 gallons per acre.

DETAILED DESCRIPTION The following examples describe the preparation of the present compounds and tests as antibacterial and antifungal agents.

EXAMPLE 1 Preparation of 5-nitro-1,3,4-thiadiazole-2- carboxaldehyde (IV) The compound Z-methyl-S-nitro-1,3,4-thiadiazole (I) (0.73 g. or 5 mmoles) and 0.55 g. (5 mmoles) of selenium dioxide are mixed and heated until a highly exothermic XVI XXIII reaction occurs. The mixture is cooled and extracted with methylene chloride. The extracts are dried and evaporated to dryness to give a red-brown liquid, which is the title compound; infrared spectrum (neat): 1700 (C=O), 1565 and 1355 (-NO cmr EXAMPLE 2 Preparation of [M5-acetamido-1,3,4-thiadiazol-2-yl)- p-nitro-styrene (II) To 157 g. 1.0 mole) of 2-acetamido-S-methylthiadiazole and 151 g. (1.0 mole) of p-nitrobenzaldehyde is added 1500 ml. of hot acetic anhydride and the mixture heated under reflux for 17 hours. The mixture is cooled, the yellow solid collected and washed thoroughly with acetone. After drying at C., for 17 hours under reduced pressure, 198.7 g. of title compound is obtained. A sample purified from dimethylformamide-acetone mix ture melts above 310 C.

EXAMPLE 3 Preparation of S-amino-1,3,4-thiadiazole-2- carboxaldehyde (III) In 700 ml. of ethyl acetate, 20 g. (0.069 mole) of ,6- (S-acetamido-1,3,4-thiadiazol-2-yl)-p-nitrostyrene is treated with ozone (4% O in 0 stream, 0.08 mole per hr.) at -30 to 35 C. for 2 hours to give a tan-colored suspension. The reaction mixture is purged of ozone with nitrogen for 20 minutes. To this, 60 g. of sodium iodide in 40 ml. glacial acetic acid and 400 ml. of water are added which are followed by 80 g. of sodium thiosulfate in 800 ml. of Water. The organic layer is separated after 500 ml. of ethyl acetate is added and the aqueous layer further extracted with 400 ml. of ethyl acetate. The extracts are dried over magnesium sulfate, filtered, and evaporated to give a yellow-brown sticky solid (20.5 g.). This material contains a mixture of p-nitrobenzaldehyde and S-acetamido-l,3,4-thiadiazole-Z-carboxaldehyde. The mixture is heated on a steam bath for 70 minutes with 19 ml. of concentrated hydrochloric acid and 20 ml. of glacial acetic acid. Evaporation of the acids under reduced pressure gives a yellow solid, which is treated with 300 ml. of 10% hydrochloric acid to dissolve the aminothiadiazole aldehyde and the mixture is extracted twice with 200 ml. volumes of ethyl acetate to remove p-nitrobenzaldehyde. The aqueous acid phase is neutralized with sodium bicarbonate and then extracted with three 300 ml. volumes of ethyl acetate. These latter extracts are combined and dried over magnesium sulfate and evaporated to give 2.3 g. of solid yellow product amino-1,3,4-thiadiazole-2-carboxyaldehyde; infrared v (Nujol): 1688 cm. (C O), NMR (acetone -d 1.831- (NH and 0.04-r (CHO).

In a similar run, liquid-liquid extraction of the final aqueous phase with ethyl acetate gives a total yield of 4.1 g. of S-amino 1,3,4-thiadiazole-2-carboxaldehyde, melting point 155157 C. (dec.).

EXAMPLE 4 Preparation of 5-nitro-1,3,4-thiadiazole-2- carboxaldehyde (IV) 1.0 g. of 5-amino-1,3,4-thiadiazole 2 carboxaldehyde is dissolved in a mixture of 2 ml. of 48-50% fluoboric acid and 5 ml. of water and added dropwise in about 20 minutes to a vigorously stirred suspension of 0.50 g. of copper powder in 2.0 g. of sodium nitrite in ml. of water. The solution becomes green, foams, and a brown-yellow solid appears. The mixture is stirred for 30 minutes, filtered, and the insoluble solid washed with 5075 ml. portions of hot chloroform until no more color is removed. The filtrate is extracted with ether (2 times with 100 ml. volumes), with 100 ml. of benzene, and with 100 ml. of chloroform. These extracts give about 0.1 g. of S-nitro-1,3,4-thiadiazole-Z-carboxaldehyde. The hot chloroform washes yield 0.60 g. of S-nitro- 1,3,4 thiadiazole 2-carboxaldehyde. These combined crude materials are dissolved in ether, filtered, and the filtrate evaporated to dryness to give 0.44 g. of purer title compound which is orange and exhibits a carbonyl band at about 1680-1700 cm. in the infrared; this material is semi-solid.

EXAMPLE 5 Preparation of 3-{ S-nitro-1,3,4-thiadiazol-2-yl)methylene]amino}-2-oxazolidinone (V) A solution of 2.1 g. (0.013 mole) of 5-nitro-2-thiadiazolecarboxaldehyde in ml. of 95% ethanol is added to a solution of 1.53 g. (0.015 mole) of 3-amino-2- oxazolidinone in 10 ml. of 95% ethanol. The resulting solution is treated with 2 drops of concentrated hydrochloric acid and heated for 15 minutes on a steam bath. The yellow solid is collected and dried to give 1.1 g., melting point 248250 C., of the title compound.

EXAMPLE 6 Preparation of 1-{[(5-nitro-1,3,4,-thiadiazo1-2-yl)methylene] amino}-2-imidazolidinone (VI) A solution of 1.8 g. (0.011 mole) of 5-nitro-1,3,4-thiadiazole-Z-carboxaldehyde in ml. of 95% ethanol is added to 40 m1. of a 0.33 M solution of l-amino-Z-imidazolidinone in dilute sulfuric acid and the mixture heated on a steam bath. Water is added to the mixture until a clear solution is obtained and after 30 minutes of heating, it is cooled. The brown needles are collected and recrystallized from 80 ml. of 67% aqueous ethanol to give 1.0 g. of yellow crystals, melting point 230-232 C. of the title compound.

EXAMPLE 7 Preparation of 5-nitro-1,3,4-thiadiazole-2-carboxald-ehyde thiosemicarbazone (VII) 5 g. (0.031 mole) of S-nitro-1,3,4-thiadiazole-2-carboxaldehyde is dissolved in 50 ml. of 95% ethanol and 3.6 g. (0.04 mole) of thiosemicarbazide in 50 ml. of 50% aqueous ethanol and 5 drops of concentrated hydrochloric acid are added. The mixture is heated at 90-95 C. for 30 minutes, cooled, and the red solid collected. The yield of the title compound, melting point 290 C., is 4.0 g.

8 EXAMPLE 8 Preparation of 2-amino-5-(5-nitro-1,3,4-thiadiazol-2-yl)- 1,3,4-thiadiazole (VIII) A suspension of 1.0 g. of 5-nitro-2-thiadiazolecarboxaldehyde thiosemicarbazone in a solution of 8.0 g. of ferric ammonium sulfate dodecahydrate in 20 ml. of water is heated at 95 C. for 2 hours, cooled, and the solid collected. The solid is recrystallized from 1:1 ethanol-acetone mixture which contains small amounts of dimethylformamide to give yellow crystals, melting point 240 C. (dec.), of the title compound.

EXAMPLE 9 Preparation of 2-methyl-5-nitro-1,3,4-thiadiazole (I) A solution of 2.78 g. (0.024 mole) of Z-methyl-S-aminothiadiazole in 17.5 ml. of 48-50% fluoboric acid is stirred at 0 C. while 1.67 g. (0.024 mole) of sodium nitrite is added over 30 minutes. The mixture is stirred for 20 minutes at 0 C. and then added dropwise to a vigorously stirred suspension of 4.9 g. of copper powder in a solution of 24.7 g. of sodium nitrite in 50 ml. of water at 25 C. The mixture is stirred for 30 minutes, filtered, and the filter cake washed thoroughly with water. The combined filtrate and washings are extracted with three 150 ml. volumes of benzene. The combined extracts are dried and evaporated under reduced pressure to give 1.75 g., melting point 54-55 C., of Z-methyl-S-nitro-1,3,4-thiadiazole.

EXAMPLE 10 Preparation of [3-(S-amino-1,3,4-thiadazo1-2-yl)-p-nitrostyrene (X) A suspension of 5.0 g. of (3-(5-acetamido-1,3,4-thiadiazol-Z-yl)-p-nitrostyrene in 20 ml. of concentrated hydrochloric acid and 20 ml. of glacial acetic acid is heated to reflux temperature for 2 hours. The solid is collected, washed with ether, and dried to afford 4.4 g. of solid. This solid is washed with 25 ml. of 5% sodium bicarbonate solution and heated to 50-55 C. until foaming stops. The solid is collected, washed with water and dried to give 0.81 g. of yellow B-(5-amino-1,3,4-thiadiazol-2-yl)-p nitrostyrene, melting point 284 C. (dec.).

EXAMPLE 11 Preparation of S-acetamido-1,3,4thiadiazole-2-carboxaldehyde (XI) A portion of 1.29 g. (0.01 mole) of 5-amino-1,3,4-thiadiazole-Z-carboxaldehyde is heated with 5 ml. of acetic anhyride at reflux temperature, cooled and evaporated to dryness. The yellow solid is washed with saturated aqueous sodium carbonate solution to afford 5-acetamido-1,3,4- thiadiazole-Z-carboxaldehyde.

EXAMPLE 12 Preparation of 1-{[(S-amino-1,3,4-thiadiazol-2-yl) methylene]amino}-2-imidazolidinone (XII) The compound S-amino-1,3,4-thiadiazole-2-carboxaldehyde (1.29 g. or 0.01 mole) is reacted with l-amino-Z- imidazolidinone in the manner described in Example 6 to give 1-{[(S-amino-l,3,4-thiadiazol 2 yl)methylene] amino}-2-imidazolidinone, which is collected as a pale yellow solid.

EXAMPLE 13 Preparation of 1-{[(5-acetamido-1,3,4- thiadiazol-2-yl) methylene] amino}-2-imidazolidinone (XIII) To 1.71 g. (0.01 mole) of S-acetamido-1,3,4-thiadiazole- 2-carboxaldehyde in 20 ml. of ethanol is added to 40 ml. of a 0.33 M solution of l-amino-Z-imidazolidinone in the manner described in Example 6 to give solid 1-{[(5- acetamido-1,3,4-thiadiazol 2 yl)methylene]amino}-2- imidazolidinone.

9 EXAMPLE 14 Preparation of 3-{ (-acetamido-1,3,4-thiadiazol-2-yl) methylene]amino}-2-oxazolidinone (XIV) The compound 3-amino-2-oxazolidinone is reacted in equimolar amounts with S-acetamido-1,3,4-thiadiazole-2- carboxaldehyde in the manner described in Example 5 to give 3-{[(S-acetamido-l,3,4-thiadiazol-2 yl)methylene] amino}-2-oxazolidinone, which is collected as an oiT-white solid.

EXAMPLE 19 Preparation of Z-acetamido-S-(S-acetamido-1,3,4-thiadiazol-2-yl)-1,3,4-thiadiazole (XIX) The compound 2-amino-5-(S-amino-l,3,4-thiadiazole- 2-yl)-1,3,4-thiadiazole is refluxed with acetic anhydride for /2 hour, evaporated to dryness, and the remaining solid Washed with saturated aqueous sodium carbonate to give the title compound.

EXAMPLE 15 EXAMPLE 2O Preparation of 2-[2-(S-nitro-1,3,4-thiadiazol-2-yl) Preparation of 3-{ (S-amrno-1,3,4:th1ad1azol-2-yl) vinyuquinoline X ff f In 3 ml. of glacial acetic acid at 60-70 c., 0.72 g.

Eqlllmolal' quantltles 5'amlno'l@cfhthladlazole (5 mmoles) of freshly distilled quinaldine and 0.8 g. (5 fial'boXaldehyde and f reacted mmole) of 5nitro-1,3,4-thiadiazole-2-carboxaldehyde are m the manner described 1n Example 5 to g v 3-{[( stirred while 0.8 ml. of acetic anhydride is added dropllP- l -Y y wise. The mixture is refluxed for 4 hours, cooled, and lolldlone, Whlch 1S Collected y filtfatlol'l as a Solidthe solvents are evaporated under reduced pressure. The

EXAMPLE 16 20 remaining solid is washed with ether and collected by filtration to give the above compound.

Preparation of S-acetamido-1,3,4-thiadiazole-2-carboxaldehyde thiosemicarbazone (XVI) EXAMPLE S-acetamido-1,3,4-thiadiazole-Z-carboxaldehyde is re- Preparation of j f f aceted with an equimolar quantity of thiosemicarbazide 25 vlnyuqulnollne in the manner described in E a p e 7 f g the 'f The title compound is prepared as described in Excompound, which 1s collected by filtration as a solid. ample 20 by reacting 5-amil10-1,3,4-thiadiazole 2 ca bo EXAMPLE 17 2151535? with quinaldine in the presence of acetic an- Preparation of S-amino-1,3,4-thiadiazolecarboxaldehyde EXAMPLE 22 thlosemlcafbalolle Preparation of 2-[2-(d-arnino-1,3,4-thiadiazol-2-yl) In 15 ml. of 95% ethanol, 1.29 g. 0.91 mole) of 5- vmynqumohne (XXII) amino-1,3,4-thiadiazole-Z-carboxaldehyde and 0.92 g. of r The above compound is obtained by treating 1 g. of thiosemicarbazide are reacted in the manner described 2 [2 (5 acetamido 1,3,4 thiadiazol 2 yl)vinyl] in Example 7 to give the above compound, which is colquinoline with 5 ml. of concentrated hydrochloric acid in lected by filtration as a solid. 5 ml. of glacial acetic acid for 2 hours on a steam bath and neutralizing the mixture with saturated aqueous sodi- EXAMPLE 18 40 um carbonate soluti0n. The solid product is collected by Preparation of 2-amino-5-(S-amino-1,3,4-thiadiaz0lfiltratlon and washed Wlth water 2-y1)-1,3,4-thiadiazole (XVII-I) A L 23 The title compound is prepared in the manner de- The antibacterial activity of the compounds of the presscnbed in Example 8 by cycllzing 2-amino-1,3,4-thiadient invention is demonstrated by the following tests whereazole-2-carboxaldehyde thlosemicarbazone and collecting in test compounds are dissolved in deionized water in the product asasolld. sufficient amount to provide p.p.m. of compound TABLE I Rate, A. aern- X.vesz'ca- Compound p.p.m. genes S.au1eus toria N.. ..N 100 9 9 9 O Nl CHa NN 100 9 5 9 O Nl CH=NN (H) 0211 CH=N-N-L 11-? 100 9 9 5 and in the water. Test solutions are then sterilized and inoculated with a bacterial cell suspension of the test organism. The bacterial cell suspensions are 24 hour broth (0.1% dextrose-1.0% peptone) cultures that were inoculated with bacteria from 7-day Nutrient Agar Slants. After exposure for 24 hours, each test solution is treated with by volume of a 1% dextrose-10% peptone broth. The treated solutions are then incubated for 24 hours at 37 C. and then examined for the presence or absence of bacterial growth. Determinations are made by turbidity readings. Solutions with no bacterial growth are subcultured to determine if the bacteria have been killed. Data are recorded as follows: 9=kill; 5=stasis; 0=no apparent effect.

Bacteria employed are Aerobacter aerogenes, a gram negative organism used by the Paper Institute to evaluate slime control agents for paper mills. Staphylococcus aureus, a gram positive common on the skins of man and animals and certain strains of which are pathogenic, and Xanthomonas vesicatoria, a gram negative organism which incites bacteriosis of tomatoes and peppers.

Data obtained are provided in Table I.

EXAMPLE 24 The antifungal activity of the compounds of the invention is demonstrated by the following test wherein 710 day cultures of M. fructicola, 14 day cultiures of S. sarcinaeforme and 7 day cultures of A. niger are separately washed from slants with deionized water and the suspensions filtered to remove large pieces of mycelium. Two ml. of orange juice are added per liter of spore suspension to facilitate germination. Opticular vials are then partially filled with the individual suspensions of test organism and a sufiicient amount of aqueous solution or suspension of test compound added to provide 100 p.p.m. thereof to the test vials. The vials are placed on a tumbler and rotated for 24 hours to expose the organisms to the test compounds. At the end of a 24 hour exposure period the suspensions are examined macroscopically. Data are recorded as percent of the spores that have not germinated and are reported below.

As indicated above the organisms used are Monilinia fructicola, the pathogen that incites American brown rot of stone fruits; Stemphylium sarcinaeforme, the pathogen which incites leaf spot of legumes and Aspergillus niger, the saprophyte that degrades textiles, fabrics, leathers, fruits and vegetables.

EXAMPLE 25 The antibacterial activity of the compounds of the present invention is further demonstrated in the following tests wherein trypticase soy agar plates are prepared containing 4 to 250 meg/ml. of test compounds.

The plates stored at room temperature overnight then are inoculated with the desired cultures. After inoculation the plates are permitted to dry, then inverted and incubated for 24 hours at 37 C. After the incubation the plates are examined and growth or no growth determi- 12 nations made by comparison with growth control plates. The results are recorded and reported below in Table III as the minimum concentration (meg/ml.) required to prevent growth of the organism. Organisms employed are recorded below.

Gram positive bacteria Abbreviation: Name 1. B.c. Bacillus cereus. 2. B.s Bacillus subtilis. 3. B.t. Bacillus thuringiensis. 4. C.x. Cornynebacterium xerosis. 5. M. Micrococcus. 6. S.a. Staphylococcus aureus. 7. S.a Streptococcus agalactiae. 8. S.f Streptococcus faecalis.

Gram negative bacteria 9'. A.a. Aerobacter aerogenes. 10. A.f Alcaligenes faecalis. 11. Rb. Bordetella bronchiseptica. 12. EC. Escherichia coli. 13. Pm. Pasteurella multocida. 14. 8.0. Salmonella choleraesuis. 15. S.d Salmonella dublin. 16. S.g. Salmonella gallinarum. 17. S.t Salmonella typhi. 18. Se. Saccharomyces cerevisiae.

TABLE III Dose, Compound meg/ml. Organisms 5-nit1'0-1,3,4-thladiazole-Z-carboxalde- 8.2., S.a.

hyde thiosemicarbazone.

3-{[(5-nitro-1,3,4-thiodiazol-2-yl) 125 3.3., C.x., A. f.,

methylene] amino }-2-oxazolidinone. Rm.

250 B.c.,B.b., 8.0., 8.9., S.l., S.a.

't' 1,3,4-tl1d" 1-2-1 31 Pan. 1 m m We y) 0.1., AL, 3.1)., S.a.

125 B.c., B.s., S.a.,

A.a., A.f., E.c., S.g., S.t., 8.0. 250 S].

-au1iuo-5-(5-nitro-l,3,4-thiadiazol-2-yl) 250 A./., Pan.

1,3,4-thiadiaz0le.

125 S.t., S.t.

What is claimed is: 1. A compound of the formula:

.ljlt.

wherein R is selected from the group consisting of amino and lower alkanoylamino.

2. The compound, S-amino-1,3,4-thiadiazole-2-carboxaldehyde.

3. The compound, S-acetamjdo-1,3,4-th1ad1azole-2-carboxaldehyde.

4. The compound, S-nitro-l,3,4-thiadiazole-2-carboxa1- dehyde.

References Cited UNITED STATES PATENTS 3,497,597 2/1970 Tomcufcik et al 260302 ALEX MAZEL, Primary Examiner R. I. GALLAGHER, Assistant Examiner U.S. Cl. X.R.

260-240D, 240E, 240G, 302H, 306.8D; 424258, 270 

